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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 435915Generated: October 30, 2026

Methylhydrazine → N-(5-Cyclohexyl-1,3,4-thiadiazol-2-yl)-1-methylhydrazine-1-carboxamide

https://huagongshe.com/reaction/435915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylhydrazineHCID 6061—
ReactantHydrazineHCID 9321—
Reactant2-Cyclohexyl-5-isocyanato-1,3,4-thiadiazoleHCID 53924444—
SolventDichloromethaneHCID 6344—
ProductN-(5-Cyclohexyl-1,3,4-thiadiazol-2-yl)-1-methylhydrazine-1-carboxamideHCID 21454603—

Reaction Steps

A solution of methylhydrazine (0.3 mole) in methylene chloride (150 ml) is charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer and reflux condenser. 5-cyclohexyl-1,3,4-thiadiazol-2-yl isocyanate dimer (0.1 mole) is then added, with stirring, at room temperature. After the addition is completed the reaction mixture is heated at reflux for a period of about 4 hours. After this time the reaction mixture is stripped of solvent and excess hydrazine to yield the desired product 2-methyl-4-(5-cyclohexyl-1,3,4-thiadiazol-2-yl)semicarbazide as the residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04007031
Source datasetuspto-grants-1977_02
ORD IDord-319a862fa58843e28fc753fafe5e3f6e
Source noteuspto-grants-1977_02